# Delta Med SpA – FDA Inspection, Oct 26, 2017

Source: https://www.keypedia.com/records/fda_inspections/delta-med-spa/ecffd11a-5eb7-4261-8c2e-28c01ea534c5
Source feed: FDA_Inspections

> FDA inspection 1029762 of Delta Med SpA, October 26, 2017. Classification: Voluntary Action Indicated (VAI). 6 citations under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1029762
- Company Name: Delta Med SpA
- Inspection Date: 2017-10-26
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 6

## Related Documents

- [FDA Inspection 1051764 - 2018-01-25](https://www.keypedia.com/records/fda_inspections/delta-med-spa/18194c00-ef75-446c-a0fe-e07cb58212b8)
- [FDA Inspection 780033 - 2012-05-03](https://www.keypedia.com/records/fda_inspections/delta-med-spa/d701ca5d-a8a7-44f5-a2f9-206a85047023)

## Related Officers

- [Company Rep](https://www.keypedia.com/people/roy-baby/69a18ef5-167c-41eb-a57e-3d138a0820c2)

Company: https://www.keypedia.com/companies/delta-med-spa/0f883efb-8062-4c4d-b9bb-d4b4f468fe6d

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7